Solvent Quality Research Articles

Solvent Quality and Aggregation State of Asphaltenes on Interfacial Mechanics and Jamming Behavior at the Oil/Water Interface.

The formation of highly stable water-in-oil emulsions results in complications in both upstream and downstream processing. Emulsion stability in these systems has been connected to the adsorption of surface-active asphaltenes that are assumed to form a rigidified film at the oil/water (o/w) interface. Full characterization of this behavior is needed to allow for engineered solutions for enhanced oil recovery. Interfacial properties, such as surface pressure and interfacial elasticity, are implicated in the stabilizing mechanism for these observed films. Asphaltenes are known to be interfacially active in both good solvents (aromatics) and poor solvents (high ratio of aliphatic to aromatic). However, due to inherent complexities present in asphaltene studies, the details of the mechanical properties of the interface remain poorly understood. Despite the widely accepted perception that asphaltenes form persistent rigid films at fluid-fluid interfaces, the connection between bulk solution properties and interfacial mechanics has not been resolved. Here, the effects of solvent quality on the interfacial properties of asphaltene dispersions are determined by using a well-defined asphaltene/solvent system. Interfacial rigidity is observed only under poor solvent conditions, while the good solvent system remains fluid-like. The interfacial rheology under good and poor solvent conditions is measured simultaneously with surface pressure measurements to track interfacial development. It is shown that surface pressure and dilatational modulus measurements are not indicators of whether an interface demonstrates rigid behavior under large compressions. Finally, conditions required for asphaltene-coated interfaces to exhibit the mechanical behavior associated with a rigidified interface are defined. This work provides a framework for quantifying the impact of the aggregation state of asphaltenes on the stability and mechanics at the o/w interface.

A quantitative evaluation of solvent quality of an environmentally friendly solvent ‘d-Limonene’ for polystyrene

A quantitative evaluation of solvent quality of an environmentally friendly solvent ‘d-Limonene’ for polystyrene

Temperature Dependence of the Gel Modulus Depends on Change of Solvent Quality

Temperature Dependence of the Gel Modulus Depends on Change of Solvent Quality

Construction of Quasi-Ordered Metal-Organic Frameworks Superstructures via Colloidal Assembly of Anisotropic Particles for Selective Organic Vapor Sensing.

Colloidal assembly of anisotropic particles holds great promise for achieving diverse packing geometries and unique photonic properties. One intriguing candidate for anisotropic self-assembly is colloidal metal-organic frameworks (MOFs), which possess remarkable characteristics including substantial surface areas, tunable chemical properties, a wide range of structural variations, and diverse polyhedral shapes. In this study, the colloidal assembly of nearly spherical and polyhedral MOFs particles to form quasi-ordered photonic superstructures was investigated. Specifically, monodisperse near-spherical ZIF-8 (NSZIF-8) and rhombic dodecahedron ZIF-8 (RDZIF-8) colloidal nanoparticles were synthesized as the fundamental building blocks. These nanoparticles are employed to construct MOFs-based self-assembled superstructures that exhibit thin-film interference optical properties. Importantly, these superstructures demonstrate exceptional responsiveness to gaseous homologues and isomers with approximate refractive indices. The dynamic reflection spectral patterns exhibited by these superstructures provide valuable insights into the diffusion rates and surface tension characteristics of the target solvents. These findings underscore the potential of MOFs-based superstructure thin films to discriminate between physiochemically similar solvents, opening new avenues for applications in various fields.

Mixing Linear Polymers with Rings and Catenanes: Bulk and Interfacial Behavior.

We derive and parameterize effective interaction potentials between a multitude of different types of ring polymers and linear chains, varying the bending rigidity and solvent quality for the former species. We further develop and apply a density functional treatment for mixtures of both disconnected (chain-ring) and connected (chain-polycatenane) mixtures of the same, drawing coexistence binodals and exploring the ensuing response functions as well as the interface and wetting behavior of the mixtures. We show that worsening of the solvent quality for the rings brings about a stronger propensity for macroscopic phase separation in the linear-polycatenane mixtures, which is predominantly of the demixing type between phases of similar overall particle density. We formulate a simple criterion based on the effective interactions, allowing us to determine whether any specific linear-ring mixture will undergo a demixing phase separation.

Crowder titrations enable the quantification of driving forces for macromolecular phase separation

Macromolecular solubility is an important contributor to the driving forces for phase separation. Formally, the driving forces in a binary mixture comprising a macromolecule dissolved in a solvent can be quantified in terms of the saturation concentration, which is the threshold macromolecular concentration above which the mixture separates into coexisting dense and dilute phases. In addition, the second virial coefficient, which measures the effective strength of solvent-mediated intermolecular interactions provides direct assessments of solvent quality. The sign and magnitude of second virial coefficients will be governed by a combination of solution conditions and the nature of the macromolecule of interest. Here, we show, using a combination of theory, simulation, and in vitro experiments, that titrations of crowders, providing they are true depletants, can be used to extract the intrinsic driving forces for macromolecular phase separation. This refers to saturation concentrations in the absence of crowders and the second virial coefficients that quantify the magnitude of the incompatibility between macromolecules and the solvent. Our results show how the depletion-mediated attractions afforded by crowders can be leveraged to obtain comparative assessments of macromolecule-specific, intrinsic driving forces for phase separation.

Hansen Solubility Parameters and QbD-Oriented HPLC Method Development and Validation for Dermatokinetic Study of a Miconazole-Loaded Cationic Nanoemulsion in Rat Model.

Miconazole (MCZ) is a potential antifungal drug to treat skin infections caused by Candida, Tinea pedis (athlete's foot fungal infection), Tinea cruris (jock itching in the groin and buttocks), and Tinea corporis (red scaly rash on the skin). The current study focused on Hansen parameter-based solvent selection (HSPiP software) and method development optimization using an experimental design tool for sensitive, accurate, reproducible, economic, rapid, robust, and precise methodology to quantify MCZ in rat plasma. Moreover, a Taguchi design was used for screening two independent factors (flow rate and ACN content). Quality by design (QbD) was employed to optimize and identify the right ratio of mobile phase composition and its impact on the peak and retention time. The elution of MCZ was achieved using methanol and acetonitrile (15:85 v/v ratio) at a retention time of 6 min and optimal flow rate (1 mL/min). Finally, the method was validated based on accuracy, precision, linearity, selectiveness, and high recovery at varied concentrations as per the International Council for Harmonization (ICH) guidelines. The method was linear (r2 = 0.999) over the explored concentration range (250-2000 ng/mL) at 270 nm detection wavelength. The optimized method was used to quantify in vivo pharmacokinetic (PK) study after transdermal application of MCZ-loaded formulations (MCNE11, MNE11, MCZ-Sol, and MCZ-MKT). HSP-oriented solvent selection and quality by design-based optimized process variables and composition in the optimized analytical methodology were quite convincing and have been a cutting-edge MCZ analysis method so far. The validated method was robust, economic, and rapid with high specificity and selectivity.

Controllable One-Step Assembly of Uniform Liquid Crystalline Block Copolymer Cylindrical Micelles by a Tailored Nucleation-Growth Process and Their Application as Tougheners.

The fabrication of uniform cylindrical nanoobjects from soft materials has attracted tremendous research attention from both fundamental research and practical application points of view but has also posed outstanding challenges in terms of their preparation. Herein, we report a one-step method to assemble cylindrical micelles (CMs) with highly controllable lengths from a single liquid crystalline block copolymer by an in situ nucleation-growth strategy. By adjusting the assembly conditions, the lengths of the CMs are controlled from hundreds of nanometers to micrometers. Several influencing factors are systematically investigated to comprehensively understand the process. Particularly, the solvent quality is found determinative in either enhancing or suppressing the nucleation process to produce shorter and longer CMs, respectively. Taking advantage of this strategy, the lengths of CMs can be nicely controlled over a wide concentration range of four orders of magnitude. Lastly, CMs are produced on decent scales and applied as additives to dramatically toughen glassy plastic matrix, revealing an unprecedented length-dependent toughening effect.

Controllable One‐Step Assembly of Uniform Liquid Crystalline Block Copolymer Cylindrical Micelles by a Tailored Nucleation‐Growth Process and Their Application as Tougheners

AbstractThe fabrication of uniform cylindrical nanoobjects from soft materials has attracted tremendous research attention from both fundamental research and practical application points of view but has also posed outstanding challenges in terms of their preparation. Herein, we report a one‐step method to assemble cylindrical micelles (CMs) with highly controllable lengths from a single liquid crystalline block copolymer by an in situ nucleation‐growth strategy. By adjusting the assembly conditions, the lengths of the CMs are controlled from hundreds of nanometers to micrometers. Several influencing factors are systematically investigated to comprehensively understand the process. Particularly, the solvent quality is found determinative in either enhancing or suppressing the nucleation process to produce shorter and longer CMs, respectively. Taking advantage of this strategy, the lengths of CMs can be nicely controlled over a wide concentration range of four orders of magnitude. Lastly, CMs are produced on decent scales and applied as additives to dramatically toughen glassy plastic matrix, revealing an unprecedented length‐dependent toughening effect.

Comparative techno-economic analysis of CO2 capture processes using blended amines

Blended amines synthesize the absorption characteristics of different amine solvents and show a great potential in carbon capture. However, a comprehensive techno-economic analysis (TEA) of the CO2 absorption process using blended amines is still lacking. In this study, we investigated three blended amine solvents: MEA/MDEA, PZ/MEA, and PZ/MDEA, with commercially available amine MEA used as the benchmark. Rigorous process simulation and techno-economic analysis were applied to evaluate the performance of the carbon capture process in a steel plant. CO2 molar loading in the lean solvent (αlean) and stripper pressure (P) were optimized to minimize the total annualized cost (TAC). The results demonstrated that PZ/MDEA-based process is most cost-effective (31.43$/tCO2) under the operating conditions of αlean = 0.15 and P = 1.25 bar. The cost breakdown analysis revealed that αlean and P significantly impact the TAC through the regeneration heat, equipment investment, and amines make-up cost. Furthermore, the energy analysis indicated that using a solvent with a low reaction enthalpy and heat capacity as well as high reactivity and absorption capacity could minimize the energy consumption of the process.

Role of concentration and hydrophobic nature of weak polyelectrolytes on adsorption structure and thermodynamics at oil-water interface: Study of several carboxylate polymers

Intermolecular structure, conformations, solvation and adsorption characteristics of four partially ionized polycarboxylic acids syndiotactic-poly(acrylic acid) (s-PAA), syndiotactic-poly(methacrylic acid) (s-PMA), isotactic-poly(methacrylic acid) (i-PMA) and atactic-poly(ethacrylic acid) (a-PEA) at oil (CCl4) - water interface is studied by molecular dynamics simulations over the range from dilute to monolayer coverage. Linearity and slope of Θ-Γ curves are correlated to conformational invariance and extent of adsorption (partial vs complete) respectively, within the range of concentration of study. Adsorption of i-PMA and a-PEA chains occurs deeper into the oil-side of interface region as driven by the greater hydrophobicity of these polymers. Higher tendency of highly extended s-PMA to desorb from the interface as compared to strong adsorption of compact coiled i-PMA is driven by their solvation behavior dictated by aspects of structural partitioning of chemical groups with respect to the solvents of the two phases. Hydrophobic side-group in the polyelectrolyte chain is responsible for the slower dynamics of the backbone. The observed variation in thickness of adsorbed layer and fractional interface coverage with concentration suggest partial adsorption of chain segments beyond saturation of interface rather than coiling of chains to accommodate additional chains. While a-PEA exhibits greater variation in interfacial tension, the change in electric potential difference across the interface indicates weak adsorption by s-PMA. The influence of the tacticity of PMA on dynamics and distribution of counter-ions is in agreement with experimental results. Results provide a significant advancement in our understanding of polyelectrolyte and polymer adsorption at oil-water liquid interface.

Electroresponse of weak polyelectrolyte brushes

End-tethered polyelectrolytes are widely used to modify substrate properties, particularly for lubrication or wetting. External stimuli, such as pH, salt concentration, or an electric field, can induce profound structural responses in weak polyelectrolyte brushes, which can be utilized to further tune substrate properties. We study the structure and electroresponsiveness of weak polyacid brushes using an inhomogeneous theory that incorporates both electrostatic and chain connectivity correlations at the Debye–Hückel level. Our calculation shows that a weak polyacid brush swells under the application of a negative applied potential, in agreement with recent experimental observation. We rationalize this behavior using a scaling argument that accounts for the effect of the surface charge. We also show that the swelling behavior has a direct influence on the differential capacitance, which can be modulated by the solvent quality, pH, and salt concentration.Graphical

Numerical simulation of the effects of non-Newtonian property of the solvent on particle suspension rheology

To investigate the effects of the non-Newtonian properties of solvents on particle suspension rheology (non-Newtonian property and viscosity), we analyzed suspension flows with different solvent characteristics. We used the power-law model to express the non-Newtonian properties of solvents. The power-law index of the suspension was denoted as nsus. and that of the solvent as [Formula: see text] to distinguish between their non-Newtonian properties. Besides, to evaluate the non-Newtonian property of the particle suspension, we estimated its power-law index [Formula: see text] by comparing its particle velocity with the velocity profile of a power-law fluid. As a result, regardless of the different area fraction, the power-law index of the particle suspension was lower than that of the solvent for [Formula: see text], 0.8, and 1.0. On the other hand, for [Formula: see text] and [Formula: see text], the power-law index of the particle suspension was higher than that of the solvent. Regarding the particle position, particles for [Formula: see text] were more concentrated on the wall side than those of the suspensions with [Formula: see text], 0.8, and 1.0. Thus, this study confirms that a change in the non-Newtonian property of a suspension due to interactions between particles and power-law fluids is an essential factor when discussing the rheology of suspensions.

The Reactivity-Enhancing Role of Water Clusters in Ammonia Aqueous Solutions.

Among the many prototypical acid-base systems, ammonia aqueous solutions hold a privileged place, owing to their omnipresence in various planets and their universal solvent character. Although the theoretical optimal water-ammonia molar ratio to form NH4+ and OH- ion pairs is 50:50, our ab initio molecular dynamics simulations show that the tendency of forming these ionic species is inversely (directly) proportional to the amount of ammonia (water) in ammonia aqueous solutions, up to a water-ammonia molar ratio of ∼75:25. Here we prove that the reactivity of these liquid mixtures is rooted in peculiar microscopic patterns emerging at the H-bonding scale, where the highly orchestrated motion of 5 solvating molecules modulates proton transfer events through local electric fields. This study demonstrates that the reaction of water with NH3 is catalyzed by a small cluster of water molecules, in which an H atom possesses a high local electric field, much like the effect observed in catalysis by water droplets [ PNAS 2023, 120, e2301206120].

Exploring the Impact of Organic Solvent Quality and Unusual Adduct Formation during LC-MS-Based Lipidomic Profiling.

Liquid chromatography-mass spectrometry (LC-MS) is the key technique for analyzing complex lipids in biological samples. Various LC-MS modes are used for lipid separation, including different stationary phases, mobile-phase solvents, and modifiers. Quality control in lipidomics analysis is crucial to ensuring the generated data's reliability, reproducibility, and accuracy. While several quality control measures are commonly discussed, the impact of organic solvent quality during LC-MS analysis is often overlooked. Additionally, the annotation of complex lipids remains prone to biases, leading to potential misidentifications and incomplete characterization of lipid species. In this study, we investigate how LC-MS-grade isopropanol from different vendors may influence the quality of the mobile phase used in LC-MS-based untargeted lipidomic profiling of biological samples. Furthermore, we report the occurrence of an unusual, yet highly abundant, ethylamine adduct [M+46.0651]+ that may form for specific lipid subclasses during LC-MS analysis in positive electrospray ionization mode when acetonitrile is part of the mobile phase, potentially leading to lipid misidentification. These findings emphasize the importance of considering solvent quality in LC-MS analysis and highlight challenges in lipid annotation.

Evaluation of Pt particles redeposition effect on gas transport in Nafion membrane

During the operation of proton exchange membrane fuel cell, Pt particles in the catalytic layer inevitably dissolve into the membrane, which affects the performance of fuel cell. In this work, molecular dynamics is employed to investigate the effect of the redeposition of Pt particles on gas diffusion and solvation characteristics in the hydration membrane. Gas diffusion, hydrophilic cluster and its connectivity are analyzed. The interaction between Pt particles, Nafion membrane and water molecules is discussed. The influence of Pt particles on the thermal conduction of membrane is also evaluated. The results demonstrate that the presence of Pt particles affects the solvation effect of membrane, leading to a weak water cluster connectivity of membrane, which in turn leads to a poor gas diffusion performance. In addition, the thermal conductivity gradually deteriorates during the redeposition of Pt particles.

Lithium Nitrate as Salt Additive for Solid Electrolyte Interphase Formation in Dual‐Ion Battery

AbstractTuning the solid electrolyte interphase (SEI) formation in dual‐ion batteries is important for improving their long‐term stability. In this context, salt additives have gained importance which can sacrificially undergo reduction thereby protecting the working salt. Herein, we have considered dual salt electrolyte models of LiNO3 additive with LiPF6 and LiFSI salt to carry out ab initio molecular dynamics (AIMD) simulations and witness the evolution of SEI layer. Various contact ion pair and solvent separated ion pair models of the dual salt electrolytes have been considered to further understand the role played by solvation shells of the ions. The small size and quicker diffusion of anions through the electrolyte results in its decomposition at the electrode surface irrespective of the anion being in contact ion pair or solvated by solvent molecules. Overall, along with underlining the role of salt additives in SEI formation, this detailed study also provides insights regarding the factors beyond solvation characteristics of salt that determines the SEI growth process.

Detection Method and Common Characteristics of Waste Solvent from Semiconductor Industry.

The recycling of organic solvents is a widely discussed topic. The waste organic solvents from thin-film-transistor liquid-crystal display (TFT-LCD) production is characterized by large quantities, multiple types, and complex compositions. Thus, the unified and compatible component analysis method is important for studying the recovery of waste organic solvents. In our work, based on the study of existing analytical methods, we designed a compatible method for the analysis of moisture using Karl Fischer analysis, for the analysis of organic compounds using gas chromatography, and for the analysis of the photoresist and other solids by evaporation. These were specific methods for analyzing the components of near-total formulation thin-film-transistor liquid-crystal display waste organic solvent. The organic matter content was analyzed via gas chromatography with a CP-Sil8CB column and flame ionization detector. The initial temperature of the column was 90 °C and the holding time was 1 min. The heating rate was 30 °C/min. The temperature was raised to 270 °C for 7 min. The internal standard method and the external standard method were used to determine the content of the main components of organic compounds. The relative standard deviation of the analytical results was 1.14~2.93%, 1.21~4.74% and 0.61%, respectively. The analytical results had good accuracy, but the external standard method was better; the recoveries were 99.76~107.60%, 95.86~107.70%, and 95.23~96.88%, respectively. Based on the composition analysis, the composition rule of the waste organic solvent was summarized. Through the exploration of the effect of the waste solvent, the common characteristics of the waste solvent were obtained. This study provides a good strategy and an optimized method for improving the efficiency of organic solvent recovery.

Size-controlled synthesis of unusual hydrogen-bonded imine-linked covalent organic framework for trypsin immobilization and drug delivery

The interlayer hydrogen-bonded, uniform, and spherical covalent organic frameworks (USCOFs) and non-hydrogen bonded, and spherical covalent organic polymers (USCOPs) were synthesized in a series of aromatic and nonaromatic solvents at room temperature. The presence of interlayer hydrogen bonds between USCOFs were investigated via electron density difference (EDD) and stacking energy calculation in various solvents by DFT methods. The in-situ mid-angle X-ray scattering measurements indicate that the (100)-plane at 0.33 Å continuously grows in USCOFs, which was absent in USCOPs. The crystalline USCOFs exhibit a high surface area of 658 m2g−1, with a pore size of 3 nm, whereas USCOPs exhibit a surface area of 16 m2 g−1 with a pore size of 19 nm. Therefore, USCOFs formation in aromatic solvents, involving solvation and reduced π–π stacking, which allow the defective intermediates to dissociate and react reversibly, leading to well-ordered molecular arrangements. These solvent characteristics are absent in nonaromatic solvents; therefore, they fail to produce well-ordered molecular arrangement, forming amorphous USCOPs. Finally, the as-synthesized USCOFs were used for a protein(trypsin)-loading and drug delivery application. In addition, the loaded protein retains its original activity. Notably, the conducted MTT assay and cellular uptake proved COF-DOX selectively killed the cancer cells rather than normal cells.

Effect of water addition on caprylic acid: Quaternary ammonium salts (QAS) deep eutectic solvents: Characterization of their structural and dynamical properties

Physicochemical properties of the binary mixtures based on Caprylic acid: Quaternary ammonium salts (QAS) (7:3 mol ratio) are investigated using MD simulations. Considering the hydrophobic character of eutectic solvents based on long-chain fatty acids, the stability of the binary mixtures was investigated in the adjacent water. In order to investigate the effect of water on intermolecular interactions in binary mixtures, the structural properties of the binary mixtures in the pure state and adjacent to water were investigated at 310 K. Assessed structural properties include the combined distribution functions (CDFs), the radial distribution functions (RDFs), the angular distribution functions (ADFs), and the Hydrogen bonding network between HBA and HBD and Spatial distribution functions (SDF). We aimed to represent the structural stability of eutectic solvents based on Caprylic acid and Quaternary ammonium salts (QAS) as a function of the alkyl chain length of cations, the evidence was found for the interaction between the chloride anion leads to the transition of HBA to the water-rich phase. The alkyl chain length of cations of Quaternary ammonium salts shows the stability of eutectic solvents in the adjacent water.